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FDA 510(k)

RADIAS FERRITIN ENZYME IMMUNOASSAY

K-Number: K933314 · 1993-09-08

ApplicantBio-Rad
Decision Date1993-09-08
Product CodeDEW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RADIAS FERRITIN ENZYME IMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1993-09-08 under 510(k) number K933314. The device is classified under product code DEW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIAS FERRITIN ENZYME IMMUNOASSAY?

RADIAS FERRITIN ENZYME IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1993-09-08. The listed applicant is Bio-Rad. The 510(k) number is K933314.

When did RADIAS FERRITIN ENZYME IMMUNOASSAY receive FDA 510(k) clearance?

RADIAS FERRITIN ENZYME IMMUNOASSAY received FDA 510(k) clearance on 1993-09-08, under 510(k) number K933314.

Who is the listed applicant for RADIAS FERRITIN ENZYME IMMUNOASSAY?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADIAS FERRITIN ENZYME IMMUNOASSAY?

The FDA product code for RADIAS FERRITIN ENZYME IMMUNOASSAY is DEW.

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Related Devices (Code: DEW)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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